Evidence map›Paper›PMID 41910425›Full record

ArticleMicrobiology spectrum2026

Lung microbiota analysis in early-stage lung adenocarcinoma.

Ke Sun, Bowen Li, Chengye Zhang, Kaichen Zhou, Zhibo Zheng, Chao Gao, Yuxiao Lin, Nan Zhang, Zhina Wang, Ji Li and 3 more

Abstract read
In one paragraph

Article in Microbiology spectrum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Ke Sun *School of Basic Medical Sciences, Institute for Immunology, Tsinghua University, Beijing, China.ORCID 0009-0002-0911-2351
Bowen Li *Department of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Chengye ZhangSchool of Basic Medical Sciences, Institute for Immunology, Tsinghua University, Beijing, China.
Kaichen ZhouBeijing Institute of Genomics, Chinese Academy of Sciences, China National Center for Bioinformation, Beijing, China.
Zhibo ZhengDepartment of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Chao GaoDepartment of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yuxiao LinDepartment of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Nan ZhangDepartment of Pulmonary and Critical Care Medicine 2, Emergency General Hospital, Beijing, China.
Zhina WangDepartment of Pulmonary and Critical Care Medicine 2, Emergency General Hospital, Beijing, China.
Ji LiDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Lan SongDepartment of Radiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Naixin LiangDepartment of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID 0000-0001-7995-4226
Zhihua LiuSchool of Basic Medical Sciences, Institute for Immunology, Tsinghua University, Beijing, China.ORCID 0000-0002-0269-0901

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung adenocarcinoma (LUAD) is a predominant subtype of lung cancer and is highly lethal. The lung tissue microbiota has been implicated in lung cancer biology but remains incompletely defined at early stages. We enrolled 40 patients with early-stage LUAD. After sequencing quality control, 34 early-stage LUAD tissues and 17 distal noncancerous lung (NC) tissues were retained, including 14 matched LUAD-NC pairs. Microbiota differences were profiled by 16S rRNA sequencing. Early-stage LUAD tissues contained more low-prevalence taxa, with higher richness metrics, but evenness-sensitive indices remained unchanged. β-Diversity analyses further supported that differences were driven primarily by the presence and absence of community membership rather than shifts in high-abundance taxa. Differential abundance analysis using MaAsLin2 identified a set of genera associated with early-stage LUAD, including IMPORTANCE: Microbial dysbiosis has been recognized as a critical factor in the development of lung cancer, but most current research has focused on the gut rather than the lung microbiota. Identifying the key microbes involved in the development of lung adenocarcinoma is therefore essential. In this study, we analyzed the composition and structure of the microbiota in early-stage lung adenocarcinoma tissues in comparison to noncancerous lung tissues. Our findings provide novel insights into the diagnostic potential of the lung microbiota in early-stage lung adenocarcinoma and enhance our understanding of its involvement in tumor progression and the discovery of potential therapeutic targets.

Indexed as

16S rRNAearly-stage lung adenocarcinomalung microbiotamicrobiota

Identifiers

PMID41910425
PMCPMC13141924

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.